A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211749



Internal ID20778789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7265289..7359150hg38UCSC Ensembl
chr4:7267016..7360877hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3893862
hg1993862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364458
Supporting Variants
Samples
Known GenesMIR4798, SORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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